| City: |
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Syracuse |
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State:
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NY |
| Zip Code: |
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13210 |
| Conditions: |
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General Anxiety Disorder, Social Anxiety Disorder |
| Purpose: |
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This study is being conducted to evaluate the safety and effectiveness of memantine Add-On
treatment of patients who are currently taking an SNRI or SSRI and who remain anxious and
symptomatic despite treatment.
Secondary objectives of this study are:
•-to evaluate if there is an improvement in disability levels following memantine dosing
-to evaluate if there is an improvement in sleep quality following memantine dosing
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| Study summary: |
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Memantine is an FDA approved treatment which helps slow down the progression of Alzheimer's
dementia.. It is felt that high glutamate levels associated with Alzheimer's dementia are
toxic to neurons which ultimately die off causing the dementia process to continue.
Memantine partially blocks the NMDA glutamate channels located on neurons in the brain.
This way, if glutamate rises, its toxic activity is blunted and neurons tend to become less
toxic and suffer less atrophy and death.
Glutamate is felt to play a role in the development of anxiety as well. Glutamate is often
in balance with another neurotransmitter, GABA. This GABA-glutamate balance (when GABA is
low and Glutamate is normal to high) is also felt to play a role in the development of GAD
or SAD. Low GABA and high glutamate levels (similar to the state of alcohol withdrawal) are
implicated in causing anxiety symptoms. Sometimes, GABA-increasing sedative drugs, such as
diazepam (Valium) are used to raise GABA activity to ward of anxiety symptoms and create a
better balance between the stimulatory glutamate and inhibitory GABA. Given memantine's
ability to lower glutamate levels, it may be able to also lower anxiety without the need for
a sedative medication. Lowering glutamate this way, may allow a patient's own GABA
concentrations to be more effective in lowering GAD or SAD symptoms.
The usual treatment in initial treatment for anxiety is to use a serotonin neurotransmitter
enhancing drug, such as paroxetine or escitalopram. These 'SSRI' drugs, unlike the
sedatives noted above, do not have addiction potential and are safer to use. In the anxiety
disorder population, only 30-70% of patients achieve full remission of anxiety symptoms when
placed on SSRI monotherapy. The usual second-line choice is to treat with a
serotonin-norepinephrine enhancing SNRI, such as venlafaxineXR in order to achieve
remission. If resistance occurs to the SNRI, to promote full anxiety symptom relief,
addition of a GABA enhancing-sedative (to raise GABA balance) to the SNRI is a reasonable
polypharmacy strategy. Sedatives, like alprazolam, are addictive and considered third line
agents now. The authors feel that memantine, given its ability to manipulate the
GABA-glutamate balance by lowering glutamate without major side effects (weight gain, sexual
problems, (ie SSRI/SNRI) nor addiction (ie sedatives) may be a reasonable add-on or
augmentation strategy to better alleviate anxiety in SNRI or SSRI partial responders.
This study is designed to evaluate generally or socially anxious patients who are only
partially responsive to typical SNRI or SSRI anti-anxiety medication therapy. Patients who
are less than 50% anxiety-alleviated on their SNRI medication will be asked to join the
study and be placed on memantine as well. This type of add-on therapy is common in
outpatient psychiatric care. This is a rater-blinded, patient open-label, non-placebo
prospective pilot study, where all subjects will receive memantine for 10 weeks. This study
would be the first to date in this treatment-resistant patient population, as the
investigators will utilize the most comprehensive set of rating scales to date in order to
best categorize patient responses in regards to anxiety with this drug. |
| Criteria: |
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Inclusion Criteria:Patients are included in the study if all of the following criteria are
met:
1. Written informed consent is obtained.
2. The patient is English-speaking and18 through 64 years of age inclusive.
3. The patient meets the DSM-IV criteria for generalized anxiety disorder or social
anxiety disorder as determined by the MINI and psychiatric evaluation.
4. The patient is currently taking venlafaxine XR- SNRI or a SSRI medication for ≥ 6
weeks and on a stable, adequate therapeutic dosage and remains anxiety symptomatic
5. The patient has a total score of at least 10 on the HAM-A scale
6. The patient has a score of at least 5 on the HADS anxiety subscale score at the
screening and baseline visits.
7. The patient has a CGI-S showing that anxiety symptom burden is impacting negatively
on subject's life
8. The patient is in good health as determined by a medical and psychiatric history,
medical examination, and cannot have major medical illness that would jeopardize
patient health during the study.
9. Women must be of nonchildbearing potential [i.e., postmenopausal, be surgically
sterile (hysterectomy or tubal ligation)] or must meet all of the following
conditions: using a reliable, medically accepted form of contraception for at least
60 days before the baseline visit, and agree to continue such use throughout the
duration of the study and for 30 days after the final dose of study drug. Reliable
forms of contraception include oral, implanted, or injected contraceptives;
intrauterine devices in place for at least 3 months; and adequate barrier methods in
conjunction with spermicide (abstinence is considered an acceptable contraceptive
regimen). Women must be given a pregnancy test (ßHCG), unless they are at least 2
years postmenopausal or surgically sterile, and the results of the test must be
negative.
10. The patient must be willing and able to comply with study restrictions and to remain
at the clinic for the required duration during the study period, and willing to
return to the clinic for the follow-up evaluation as specified in this protocol.
Patients are included in the study if all of the following criteria are met:
1. Written informed consent is obtained.
2. The patient is English-speaking and18 through 64 years of age inclusive.
3. The patient meets the DSM-IV criteria for generalized anxiety disorder or social
anxiety disorder as determined by the MINI and psychiatric evaluation.
4. The patient is currently taking venlafaxine XR- SNRI or a SSRI medication for ≥ 6
weeks and on a stable, adequate therapeutic dosage and remains anxiety symptomatic
5. The patient has a total score of at least 10 on the HAM-A scale
6. The patient has a score of at least 5 on the HADS anxiety subscale score at the
screening and baseline visits.
7. The patient has a CGI-S showing that anxiety symptom burden is impacting negatively
on subject's life
8. The patient is in good health as determined by a medical and psychiatric history,
medical examination, and cannot have major medical illness that would jeopardize
patient health during the study.
9. Women must be of nonchildbearing potential [i.e., postmenopausal, be surgically
sterile (hysterectomy or tubal ligation)] or must meet all of the following
conditions: using a reliable, medically accepted form of contraception for at least
60 days before the baseline visit, and agree to continue such use throughout the
duration of the study and for 30 days after the final dose of study drug. Reliable
forms of contraception include oral, implanted, or injected contraceptives;
intrauterine devices in place for at least 3 months; and adequate barrier methods in
conjunction with spermicide (abstinence is considered an acceptable contraceptive
regimen). Women must be given a pregnancy test (ßHCG), unless they are at least 2
years postmenopausal or surgically sterile, and the results of the test must be
negative.
10. The patient must be willing and able to comply with study restrictions and to remain
at the clinic for the required duration during the study period, and willing to
return to the clinic for the follow-up evaluation as specified in this protocol.
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Exclusion Criteria: Patients are excluded from participating in this study if 1 or more
of the following criteria are met:
1. The patient is on more than one antidepressant or anxiolytic as a standing dose. PRN
use of anxiolytic or sleeping agents may be continued at discretion of the
investigator
2. The patient has an active substance misuse disorder
3. The patient is a significant risk of suicide
4. The patient has recently started psychotherapy or counseling (within last 6 weeks)
5. The patient has other psychiatric Axis-I disorders as a principal diagnosis (except
generalized anxiety) within 6 months of screening and baseline visits; any history of
OCD, psychotic disorder, bipolar disorder, mental retardation, or clear personality
disorder. Patient may have a co-morbid substance misuse, depressive or anxiety
disorder if it has been in remission for at least 6 months prior to screening visit.
6. The patient has previously participated in any clinical study are has been treated
with memantine or venlafaxine XR.
7. The patient has used an investigational drug within 1 month before the screening
visit or is participating in a concurrent clinical trial.
8. The patient has any disorder that may interfere with drug absorption, distribution,
metabolism, or excretion (including gastrointestinal surgery).
9. The patient is unlikely to comply with the study protocol, be unreliable in providing
ratings, or is unsuitable for any reason, as judged by the investigator.
10. The patient has a clinically significant deviation from normal in the physical
examination.
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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September 22, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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